Canonical Allele Identifier: CA413664706
Gene: NEXMIF HGNC NCBI

Linked Data

gnomAD v4: X-74740749-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74740749A>G , CM000685.2:g.74740749A>G GRCh38
NC_000023.10:g.73960584A>G , CM000685.1:g.73960584A>G GRCh37
NC_000023.9:g.73877309A>G NCBI36
NG_027726.1:g.189704T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000055682.12:c.3808T>C MANE Select ENSP00000055682.5:p.Ser1270Pro
ENST00000616200.2:c.3808T>C ENSP00000480284.1:p.Ser1270Pro
ENST00000642681.2:c.3808T>C ENSP00000495800.1:p.Ser1270Pro
ENST00000055682.10:c.3808T>C ENSP00000055682.5:p.Ser1270Pro
ENST00000616200.1:c.3808T>C ENSP00000480284.1:p.Ser1270Pro
NM_001008537.2:c.3808T>C NP_001008537.1:p.Ser1270Pro
XM_011530935.1:c.3808T>C XP_011529237.1:p.Ser1270Pro
NM_001008537.3:c.3808T>C MANE Select NP_001008537.1:p.Ser1270Pro